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A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein
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نویسنده
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zhou q. ,wang h. ,chae j. ,yang d. ,demirkaya e. ,stoffels m. ,takeuchi m. ,chen c. ,ombrello a. ,schwartz d. ,hoffmann p. ,stone d. ,laxer r. ,royen-kerkhof a.v. ,ozen s. ,gadina m. ,kastner d. ,aksentijevich i.
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منبع
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pediatric rheumatology - 2015 - دوره : 13 - شماره : 1
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چکیده
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[no abstract available]
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آدرس
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nhgri/nih,bethesda, United States, nhgri/nih,bethesda, United States, nhgri/nih,bethesda, United States, nhlbi/nih,bethesda, United States, institute of health sciences,ankara, Turkey, nhgri/nih,bethesda, United States, nhgri/nih,bethesda, United States, nhgri/nih,bethesda, United States, nhgri/nih,bethesda, United States, niams/nih,bethesda, United States, nhgri/nih,bethesda, United States, nhgri/nih,bethesda, United States, the hospital for sick children,toronto, Canada, universitair medisch centrum utrecht,utrecht, Netherlands, hacettepe university,ankara, Turkey, niams/nih,bethesda, United States, nhgri/nih,bethesda, United States, nhgri/nih,bethesda, United States
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Authors
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